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Hydroxyapatite
Kinds of Hydroxyapatite Terms modified by Hydroxyapatite Selected AbstractsPhase Relations Between ,-Tricalcium Phosphate and Hydroxyapatite with Manganese(II): Structural and Spectroscopic PropertiesEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 7 2006Isaac Mayer Abstract The preparation of Mn-containing ,-tricalcium phosphate (,-TCP) samples was achieved in two ways: a) transformation of precipitated Mn-containing calcium hydroxyapatite (HA) to ,-TCP by heating at 1100 °C, and b) preparation by solid-state reaction of a mixture of CaCO3, (NH4)2HPO4, and Mn(NO3)2 at 1100 °C. Powder X-ray diffraction (XRD) analyses of the samples, obtained by both methods, show well-defined patterns with structural data of the rhombohedral R3c, ,-TCP phase. The calculated lattice constants are smaller than those known for ,-Ca3(PO4)2 because of substitution of Ca2+ by Mn2+. EPR spectroscopy indeed reveals that manganese is divalent in the samples. Apparently, the Ca(5) site in the ,-TCP structure is occupied by Mn2+. The distribution of Mn2+ between the ,-TCP and the HA phase in the case of preparation (b) was studied by EPR spectroscopy, and a pronounced preference for the former lattice was found. Micron- and submicron-sized crystals with visible faces were observed by TEM in the case of ,-TCP prepared by solid-state reaction, and large micron-sized, droplike-shaped crystals, sensitive to beam radiation, were found in the case of samples prepared by heating HA at elevated temperatures. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006) [source] Effect of Silicate-Substitution on Attachment and Early Development of Human Osteoblast-Like Cells Seeded on Microporous Hydroxyapatite Discs,ADVANCED ENGINEERING MATERIALS, Issue 1-2 2010Katharina Guth Hydroxyapatite (HA) is a well-established graft material used in bone repair. Silicon-substituted hydroxyapatite (SA; 0.8,wt% Si) has shown greater bone ingrowth and bone coverage than phase pure HA. To assess the effect of microporosity on sensitivity of cell attachment to surface physiochemistry, microporous SA and HA discs, and control Thermanox (TMX) discs were incubated with osteoblast-like cells (5,×,104 HOS-TE85 cells) under differing tissue culture conditions. To investigate early cellular attachment, organization, and differentiation, cells were also stained for integrin,,5,1, actin, and runt-related transcription factor (RUNX-2), respectively, after incubation on HA, SA, and TMX discs for 3 days. No significant differences emerged between HA, SA, and TMX discs in mean numbers of cells attached in serum free medium (SFM) over 90,min incubation. In contrast, significantly more cells were attached to SA than HA after 180,min incubation in complete medium (C-MEM) containing fetal calf serum (p,<,0.05). Cell attachment to SA and HA discs pre-conditioned in SFM supplemented with fibronectin (FN) was lower than discs pre-conditioned in C-MEM, suggesting sensitivity of an active FN conformation to the presence of co-adsorbates. Confocal microscopy demonstrated significantly more co-localization of integrin ,5,1 and actin on SA than HA. Translocalization of RUNX-2 to the nucleus was stronger in cells incubated on SA. Microporosity did not diminish the effect of surface physiochemistry on cell adhesion, and enhanced cell attachment for SA appears to be mediated by differences in the quality of adsorbed protein rather than via direct effects of substrate chemistry. [source] Electrolytic Deposition of Hydroxyapatite Coating on CoNiCrMo SubstratesADVANCED ENGINEERING MATERIALS, Issue 1-2 2010Dong-Yang Lin Hydroxyapatite (HA) coating was fabricated on CoNiCrMo alloy by electrolytic deposition (ELD). Different kinds of uncharged substrates were placed close to the cathode separately during the ELD process. Both CoNiCrMo and uncharged substrates were covered with uniform HA coatings composed of hexagonal prism crystals after 60,min deposition. The pH value of the bulk solution changed hardly while the local pH had a sharp increase after ELD. The results demonstrate the local pH plays a crucial role in the ELD process. [source] Hydroxyapatite/SiO2 Composites via Freeze Casting for Bone Tissue Engineering,ADVANCED ENGINEERING MATERIALS, Issue 11 2009Silke Blindow Freeze casting is a fabrication method that allows producing near-net-shaped ceramics with variable porosity. Hydroxyapatite (HA) was modified by the addition of different amounts of SiO2 nanoparticles during freeze cast preparation. The addition of SiO2 introduced a partial phase transformation of HA to , -tricalcium phosphate and improved the form stability due to less shrinkage after sintering. The impact of surface roughness of pure HA ceramics and the influence of SiO2 introduction during freeze casting on adhesion, proliferation, and differentiation of human osteoblast-like cells (MG-63) was investigated. While both cell attachment and proliferation of smooth pressed HA was significantly enhanced compared to rough freeze cast HA, the addition of SiO2 improved the cell numbers of the latter. The expression of cell differentiation markers osteocalcin and collagen I was found to be supported by rough surfaces (Ra,=,5,6,µm) in particular on ceramics containing SiO2 [source] Hydroxyapatite/Bioactive Glass Films Produced by a Sol,Gel Method: In Vitro BehaviorADVANCED ENGINEERING MATERIALS, Issue 11 2009Nihat C. Köseo Abstract Hydroxyapatite (HA) and HA/bioactive glass (49S) films were deposited on Si(100) substrates by a sol,gel dip-coating method. The microstructure and in vitro bioactivity of the films were investigated by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and X-ray photoelectron spectroscopy (XPS). Polycrystalline HA and amorphous bioactive glass films were obtained after annealing at 600 and 400,°C, respectively. The crystallization temperature of HA was determined to be around 568,°C. The surfaces of the HA films were covered with an apatite layer consists of spherulites formed by nanosized needle-like aggregates after the soaking in simulated body fluid (SBF) for 10 days, while amorphous HA/bioactive glass surface was covered with larger spherical crystallites. Both XPS and EDS results obtained from HA/bioactive glass film, after soaking in SBF, showed increasing P amounts on the surface at the expense of Si. The higher density of the newly formed layer on HA/bioactive glass surface than that of the HA surface after 10 days of soaking was evidence of increased reaction rate and apatite forming ability when bioactive glass layer is present on the HA films. [source] Interaction of Osteoblasts with Macroporous Scaffolds Made of PLLA/PCL Blends Modified with Collagen and Hydroxyapatite,ADVANCED ENGINEERING MATERIALS, Issue 8 2009Halil Murat Aydin To mimic natural bone, a tissue engineering scaffold was developed that combines inorganic and organic components of natural bone, its pore diameter, and its interconnected structure. Collagen was coated onto a PLLA/PCL scaffold and hydroxyapatite particles were delivered throughout the polymer matrix much more easily than with other techniques thanks to the porosity-forming method of combining two porogens, namely, salt leaching and supercritical CO2 extraction. Compared with other coating techniques, this procedure can be performed readily and homogeneous 3D hydroxyapatite coating was achieved. [source] A Short-Term Bioresorbable Bone Filling Material Based on Hydroxyapatite, Chitosan, and Oxidized Starch Tested in a Novel Orthotopic Metaphyseal Mouse Model,ADVANCED ENGINEERING MATERIALS, Issue 8 2009Elias Volkmer Despite significant advances in orthopedic surgery, no perfect bioresorbable bone-filling material has yet been clinically established. A new candidate material based on hydroxyapatite, chitosan and oxidised starch, which has the potential to covalently bind to bone in a watery milieu was tested in a new murine model. A special focus lies on the in vivo biocompatibility and bioresorbability of the new material. [source] Microstructural Engineering of Hydroxyapatite Membranes to Enhance Proton ConductivityADVANCED FUNCTIONAL MATERIALS, Issue 24 2009Dongxia Liu Abstract A new approach to enhancing proton conductivity of ceramics is demonstrated by aligning proton conductive pathways and eliminating resistive grain boundaries. Hydroxyapatite (HAP) membranes are synthesized by multistage crystallization onto palladium. The synthesis involves three steps: electrochemical deposition of HAP seeds, secondary hydrothermal crystallization onto the seed layer to promote c -axis growth normal to the substrate, and tertiary hydrothermal crystallization to promote a- axis growth to fill the gaps between the aligned crystals. The c -axis alignment with crystal domains spanning the membrane thickness significantly enhances proton conduction since protons are primarily transported along the c -axes of HAP crystals. The novel HAP membranes display proton conductivity almost four orders of magnitude higher than traditional sintered HAP ceramics. The HAP membranes on palladium hydrogen membrane substrates hold promise for use in intermediate-temperature fuel cells, chemical sensors, and other devices. The synthesis approach presented may also be applied to other ion-conducting membrane materials to enhance transport properties. [source] Bioactivity of novel carboxymethyl chitosan scaffold incorporating MTA in a tooth modelINTERNATIONAL ENDODONTIC JOURNAL, Issue 10 2010R. Budiraharjo Budiraharjo R, Neoh KG, Kang ET, Kishen A. Bioactivity of novel carboxymethyl chitosan scaffold incorporating MTA in a tooth model. International Endodontic Journal, 43, 930,939, 2010. Abstract Aim, To characterise the bioactivity of a novel carboxymethyl chitosan (CMCS) scaffold with and without incorporating mineral trioxide aggregate (MTA) in a tooth model. Methodology, Cross-linked CMCS scaffold (CaC) and MTA-coated CaC (CaMT) scaffold were prepared by freeze-drying. The bioactivity of the scaffolds was tested in vitro in four different mineralisation solutions (bulk system) and ex vivo in simulated body fluid (SBF) in the tooth model. After mineralisation, the mineral deposits on the scaffolds were analysed using scanning electron microscopy, energy dispersive X-ray, and inductively coupled plasma mass spectroscopy. All data were statistically analysed using the two-sample t -test (P < 0.05). Results, Hydroxyapatite (HAP) deposition was observed on CaC and CaMT scaffolds after 1 week of mineralisation in the tooth model and in the bulk system. The deposition was significantly higher (P < 0.05) on CaMT scaffold than that on CaC scaffold. The amount of HAP formed in the tooth model was significantly lower (P < 0.05) than that in the bulk solution. Conclusions, The CMCS scaffolds are bioactive and capable of biomineralisation by forming HAP within a tooth model ex vivo. The bioactivity of the CMCS scaffold can be enhanced by incorporating MTA. [source] Cell Proliferation of Human Fibroblasts on Alumina and Hydroxyapatite-Based Ceramics with Different Surface Treatments,INTERNATIONAL JOURNAL OF APPLIED CERAMIC TECHNOLOGY, Issue 2 2010Juliana Marchi Biocompatibility is an important characteristic of dental implant material, and in vitro tests are required to elucidate the interaction between these materials and human tissues. Cell proliferation assays were done with fibroblasts plated on the surface of alumina and hydroxyapatite sintered samples, each with a different surface treatment (sintered, rectified, or polished). After 1, 2, and three days, the samples were prepared for scanning electron microscopy observations. The data were compared by analysis of variance followed by Tukey's test. It was concluded that neither the hydroxyapatite or alumina substrate is cytotoxic, and hydroxyapatite is more biocompatible than alumina. [source] Preparation of Nano Carbonate-Substituted Hydroxyapatite from an Amorphous PrecursorINTERNATIONAL JOURNAL OF APPLIED CERAMIC TECHNOLOGY, Issue 5 2008Yanbao Li Carbonated amorphous calcium phosphate (CACP) precursors were precipitated by the wet chemical method at 5°C in the presence of poly(ethylene glycol) and carbonates. The nano carbonate-substituted hydroxyapatite (HAp) was obtained after heat treat CACP precursors at a low temperature (800°C) for 3 h. The calcium phosphates were investigated by X-ray diffraction, Fourier transform infrared spectroscopy, inductively coupled plasma, thermal gravimetric and differential thermal analysis, transmission electron microscopy, and scanning electron microscopy. The results show that calcium phosphate particles with a Ca/P molar ratio of 1.73 are AB-type carbonate-substituted HAp with about 50 nm in diameter. [source] Biodegradation and Cytocompatibility Studies of a Triphasic Ceramic-Coated Porous Hydroxyapatite for Bone Substitute ApplicationsINTERNATIONAL JOURNAL OF APPLIED CERAMIC TECHNOLOGY, Issue 1 2008Annie John Bone defects due to trauma or disease have led to the need for biomaterials as substitutes for tissue regeneration and repair. Herein, we introduce a porous triphasic ceramic-coated hydroxyapatite scaffold (HASi) for such applications. Interestingly, in the degradation experiments with isotonic buffer, HASi showed a significant release of silica with the disappearance of the tricalcium phosphate phase. Furthermore, the material also exhibited cytocompatibility with cultured bone marrow-derived mesenchymal stem cells of human origin. The material chemistry, together with the favorable cellular characteristics, indicates HASi as a promising candidate for critical-size bony defects, which still remains a formidable clinical challenge in the orthopedic scenario. [source] Controlling the biodegradation rate of magnesium using biomimetic apatite coatingJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 2 2009Yajing Zhang Abstract Magnesium is light, biocompatible and has similar mechanical properties to natural bone, so it has the potential to be used as a biodegradable material for orthopedic applications. However, pure magnesium severely corrodes in a physiological environment, which may result in fracture prior to substantial tissue healing. Hydroxyapatite (HA) is the main composition of natural bone. It has excellent bioactivity and osteoconductivity. In this study, HA coating with two different thicknesses was applied onto the surface of pure magnesium substrates using a biomimetic technique. The corrosion rate of the surface-treated substrates was tested. It was found that both types of coatings substantially slowed down the corrosion of the substrate, and the dual coating was more effective than the single coating in hindering the degradation of the substrate. Thus, the corrosion rate of magnesium implants can be closely tailored by adjusting apatite coating thickness and thereby monitoring the release of magnesium ions into the body. © 2008 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2009 [source] In vivo evaluation of hydroxyapatite foamsJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 4 2002P. Sepulveda Abstract Hydroxyapatite (HA) is widely applied as bone graft material due to its osteoconductive potential and well-established biocompatibility. In this work, macroporous hydroxyapatite structures made through foaming of aqueous suspensions and gelcasting were tested for in vivo osteointegration. These foams are composed of a three-dimensional array of spherical pores with diameters of approximately 100,500 ,m, interconnected by windows of smaller size in the range of 30,120 ,m. The HA foams were implanted in the tibia of albino New Zealand rabbits and removed after a period of 8 weeks. Histological analysis revealed that the pores in the foams were partially or completely filled progressively with mature new bone tissue and osteoid after the implanted period. No immune or inflammatory reactions were detected. The high osteoconductive potential of the HA foams provides a potential structure for use as bone substitute in orthopedic, oral, and cranio-maxillofacial reconstructive surgery, and as dento-alveolar implants. © 2002 Wiley Periodicals, Inc. J Biomed Mater Res 62: 587,592, 2002 [source] An ultrastructural study of cellular response to variation in porosity in phase-pure hydroxyapatiteJOURNAL OF MICROSCOPY, Issue 2 2004B. ANNAZ Summary Hydroxyapatite has been shown to be biocompatible and bioactive. Incorporation of porosity has been shown to enhance osteointegration; however, difficulty in controlling the extent and type of porosity has limited investigation into determining the role of both macro- and microporosity. The current investigation reports on the synthesis of four types of phase-pure hydroxyapatite with varying levels of porosity (HA1,HA4), and with defined levels of macro- and microporosities. Transmission electron microscopy was used to evaluate qualitatively the effect of these two parameters on cell,material interactions following a 30-day incubation period. Biological mineralization was observed within vesicles and the needle-like minerals were confirmed as hydroxyapatite using X-ray microanalysis. This demonstrated the suitability of primary human osteoblast-like cells as a tool to assess the extent of mineralization. Furthermore, internalization of hydroxyapatite particles was observed. Our findings show that the variation in macro- and microporosity does not affect the extent of cell,material interaction, with collagen synthesis evident in all samples. [source] Deposition of Carbonated Hydroxyapatite (CO3HAp) on Poly(Methylmethacrylate) Surfaces by Decomposition of Calcium,EDTA ChelateJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 10 2008Yusuf Yusufoglu Inspired from the nature, the development of organic,inorganic composites between polymers and hydroxyapatite (HAp) has been investigated extensively. In this study, bone-like apatite (carbonated hydroxyapatite, CO3HAp) was precipitated on poly(methylmethacrylate) (PMMA) films by the oxidative decomposition of Ca,EDTA (calcium,ethylenediamine tetraacetate) chelates. Corona-treated PMMA films were soaked in a Ca,EDTA,PO4,H2O2 solution and aged at 63°C and pH,9 for times ranging from 1 to 24 h. Apatite formed on PMMA films was characterized by X-ray diffraction, Fourier transform infrared (FTIR), Scanning electron microscope, energy-dipersive X-ray spectroscopy, and carbon analysis. The apatite was found to be CO3HAp with Ca/P atomic ratio ranging between 1.3 and 1.9. Elemental analyses indicated that the carbonate content of the apatite phase was around 6.5 wt% after 24 h of aging time. Lattice parameters were estimated using a Rietveld profile-analysis and found to be a=0.9438 nm and c=0.6901 nm. Furthermore, FTIR spectra indicated that the apatite deposited on PMMA was B-type CO3HAp, in which carbonate ions occupy the phosphate sites. In the first 3 h of aging, isolated rod-like HAp particles were observed. With time, the needle-like crystallites radiate from a nucleus to form double-spherulite shape particles. The crystallites grew into a continuous layer with a thickness of ,15 ,m after 24-h aging. The adhesive strength between the PMMA substrate and the apatite layer was determined to be around 1.7 MPa. [source] Conversion of Bioactive Borosilicate Glass to Multilayered Hydroxyapatite in Dilute Phosphate SolutionJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 12 2007Yadong Li The conversion of a bioactive borosilicate glass in aqueous phosphate solution was observed to produce vastly different reaction kinetics and hydroxyapatite (HA) microstructures, depending on whether the glass was reacted continuously or intermittently in the solution. Particles (150,300 ,m) of a borosilicate glass (designated H12) were reacted continuously or intermittently in 0.25M K2HPO4 solution with a starting pH value of 7.0 at 37°C. The conversion kinetics of the glass particles to HA were determined from weight loss measurements. Structural and compositional changes resulting from the conversion reaction were characterized using scanning electron microscopy, X-ray diffraction, energy-dispersive X-ray analysis, and Fourier transform infrared spectroscopy. For conversion experiments carried out intermittently (12,24 h intervals, followed by drying), faster reaction kinetics and a unique multilayered microstructure, consisting of alternating layers of HA and an amorphous SiO2 -rich material with nearly uniform thickness (2,3 ,m), were observed. On the other hand, particles reacted continuously in the phosphate solution for the same total time converted more slowly and produced a single HA layer. The kinetics and mechanism of forming HA under the intermittent and continuous reaction conditions are described and compared with those for bioactive silicate and borate glasses studied in previous work. [source] Reaction Sintering and Mechanical Properties of Hydroxyapatite,Zirconia Composites with Calcium Fluoride AdditionsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 6 2002Hae-Won Kim The effects of calcium fluoride (CaF2) additions on the densification and mechanical properties of hydroxyapatite,zirconia composites (HA,ZrO2) were investigated. When small amount of CaF2 was added, the density of the composites was markedly enhanced. The reactions of HA with CaF2, which led to the formation of fluorapatite (FA), were attributed to the observed improvements in densification. When HA,20-vol%-ZrO2 composites were sintered, with the addition of 5 vol% of CaF2, in air at 1300°C, the density of the specimen approached 98% of the theoretical value. The flexural strength and fracture toughness of the composites were also improved, as a result of the enhanced densification. [source] Hydroxyapatite as a filler for biosynthetic PHB homopolymer and P(HB,HV) copolymersPOLYMER INTERNATIONAL, Issue 7 2003Antje Bergmann Abstract This paper deals with some of the fundamental problems encountered when using a semicrystalline polymer as the matrix phase for a particulate-filled composite. As our model system we adopted poly-(R)-3-hydroxybutyrate, PHB, and two copolymers of (R)-3-hydroxybutyrate and (R)-3-hydroxyvalerate, P(HB,HV), for the matrix phase, and the mineral calcium hydroxyapatite as a particulate filler. The structure and properties of compression-moulded films of various compositions were investigated by polarized light microscopy, wide-angle X-ray scattering and mechanical testing. It was found that the degree of crystallinity of the matrix was lower in filled samples, and that the spherulitic crystallization of the matrix appeared to cause the filler particles to form agglomerates, which would not be as effective a reinforcement as finely dispersed primary filler particles. The tensile strength, strain-to-break and tensile modulus of samples of different compositions were analysed using well-known theories for composite behaviour. Copyright © 2003 Society of Chemical Industry [source] Comparative proteomics profile of osteoblasts cultured on dissimilar hydroxyapatite biomaterials: An iTRAQ-coupled 2-D LC-MS/MS analysisPROTEINS: STRUCTURE, FUNCTION AND BIOINFORMATICS, Issue 20 2008Jinling Xu Dr. Abstract Hydroxyapatite (HA) and its derived bioceramic materials have been widely used for skeletal implants and/or bone repair scaffolds. It has been reported that carbon nanotube (CNT) is able to enhance the brittle ceramic matrix without detrimental to the bioactivity. However, interaction between osteoblasts and these bioceramics, as well as the underlying mechanism of osteoblast proliferation on these bioceramic surfaces remain to be determined. Using iTRAQ-coupled 2-D LC-MS/MS analysis, we report the first comparative proteomics profiling of human osteoblast cells cultured on plane HA and CNT reinforced HA, respectively. Cytoskeletal proteins, metabolic enzymes, signaling, and cell growth proteins previous associated with cell adhesion and proliferation were found to be differentially expressed on these two surfaces. The level of these proteins was generally higher in cells adhered to HA surface, indicating a higher level of cellular proliferation in these cells. The significance of these findings was further assessed by Western blot analysis. The differential protein profile in HA and CNT strengthened HA established in our study should be valuable for future design of biocompatible ceramics. [source] In Vivo Osteogenic Capability of Human Mesenchymal Cells Cultured on Hydroxyapatite and on ,-Tricalcium PhosphateARTIFICIAL ORGANS, Issue 6 2009Asako Matsushima Abstract The aim of the current study was to examine in vitro osteogenic capability and in vivo bone formation of mesenchymal stromal cells (MSCs) on two kinds of calcium phosphate ceramics. MSCs derived from human bone marrow were seeded on either hydroxyapatite (HA) ceramic or ,-tricalcium phosphate (,-TCP) ceramic and then cultured in a medium supplemented with a donor's serum, vitamin C, ,-glycerophosphate, and dexamethasone. The culture revealed the expression of alkaline phosphatase activity, indicating the osteogenic differentiation of the MSCs on the ceramics (fabrication of tissue-engineered construct). The constructs were then implanted subcutaneously into nude rats for 8 weeks. New bone formation was observed in both types of ceramics, and human-specific Alu sequence was detected by in situ hybridization analysis. Quantitative microcomputed tomography showed that the volume of the new bone in the HA ceramic was greater than that in the ,-TCP ceramic in six of seven cases. These results suggest that human MSCs cultured on ceramics could retain their osteogenic capability even after ectopic implantation and provide a rationale for the use of tissue-engineered constructs derived from a patient's MSCs and calcium phosphate ceramics in bone tissue regeneration. [source] A Molecular Dynamics Simulation Study of (OH - ) Schottky Defects in Hydroxyapatite.CHEMINFORM, Issue 27 2005Dirk Zahn No abstract is available for this article. [source] Atomistic Simulation Study of the Order/Disorder (Monoclinic to Hexagonal) Phase Transition of Hydroxyapatite.CHEMINFORM, Issue 25 2005Oliver Hochrein No abstract is available for this article. [source] A 5-Year Prospective Follow-Up Study of Implant-Supported Fixed Prostheses in Patients Subjected to Maxillary Sinus Floor Augmentation with an 80:20 Mixture of Bovine Hydroxyapatite and Autogenous BoneCLINICAL IMPLANT DENTISTRY AND RELATED RESEARCH, Issue 2 2004Mats Hallman DDS ABSTRACT Background: Prospective long-term follow-up studies evaluating the use of bone substitutes to enable dental implant placement and integration are rare. Purpose: This study was undertaken to evaluate the survival rate of dental implants placed 6 months after maxillary sinus floor augmentation using a mixture of 80% bovine hydroxyapatite (BH) and 20% autogenous bone (AB). Material and Methods: Twenty patients subjected to 30 maxillary sinus floor grafting procedures using fibrin glue and an 80:20 mixture of BH and AB to enable placement of dental implants 6 months later were followed for 5 years of functional loading. Clinical and radiographic examinations of the grafts and implants were performed. Results: After 5 years of functional loading with fixed bridges, 15 of 108 implants had been lost, giving a cumulative survival rate of 86%. The mean marginal bone loss after 5 years was 1.3 ± 1.1 mm. Conclusion: Grafting of the maxillary sinus with a mixture of BH and AB and later placements of turned implants could be performed with predictable long-term results. All but one of the patients who were observed had functional fixed bridges after 5 years of functional loading. [source] Histologic Analysis of Clinical Biopsies Taken 6 Months and 3 Years after Maxillary Sinus Floor Augmentation with 80% Bovine Hydroxyapatite and 20% Autogenous Bone Mixed with Fibrin GlueCLINICAL IMPLANT DENTISTRY AND RELATED RESEARCH, Issue 2 2001Mats Hallman DDS Abstract: Background: Bovine hydroxyapatite (Bio-Oss®, Geistlich Pharmaceutical, Wollhausen, Switzerland) has been suggested to be used in maxillary sinus floor augmentation procedures prior to or in conjunction with implant placement. However, the long-term histologic fate of this material is not well understood. Purpose: The aim with this study was to histologically evaluate the tissue response in patients to a mixture of bovine hydroxyapatite (BH), autogenous bone, and fibrin glue 6 months and 3 years after a maxillary sinus floor augmentation procedure. Materials and Method: Biopsies were taken from a group of 20 consecutive patients 6 months (n = 16) and 3 years (n = 12) after maxillary sinus floor augmentation with a mixture of BH (80%), autogenous bone (20%), and fibrin glue and prepared for histologic analysis. Results: Light microscopy and morphometry from biopsies taken after 6 months showed various amounts of mineralized bone tissue. The specimen area was occupied by 54.1 ± 12.6% nonmineralized tissue, followed by 21.2 ± 24.5% lamellar bone, 14.5 ± 10.3% BH particles, and 10.2 ± 13.4% woven bone. The nonmineralized tissue seen in bone-forming areas consisted of a loose connective tissue, rich with vessels and cells. There were no signs of resorption of the BH particles. The lamellar bone appeared to have originated from the recipient site and was seldom in contact with the BH particles. After 3 years, the nonmineralized tissue area had decreased to 36.0 ± 19.0% (p > .05) and consisted mainly of bone marrow tissue. The surface area of lamellar bone had increased to 50.7 ± 22.8% (p > .05), and there was almost no immature bone. The mean specimen area occupied by BH particles, was 12.4 ± 8.7% and had not changed from 6 months (not significant). Moreover, the sizes of the particles were similar after 6 months and 3 years. The degree of BH particle,bone contact had increased from 28.8%± 19.9% after 6 months to 54.5 ± 28.8% after 3 years (p > .05). Conclusion: Histology of specimens from maxillary sinuses augmented with 80% BH particles, 20% autogenous bone, and fibrin glue showed a positive bone tissue response after 6 months and 3 years after augmentation of the maxillary sinus floor prior to implant placement in a group fo 20 patients. The bone surrounding and in contact with the BH particles after 6 months was mainly immature woven bone, which with time was replaced by mature lamellar bone filling the interparticle space as observed in the 3-year specimens. Moreover, bone-integrated BH particles seem to be resistant to resorption. The results indicate that the procedure may be considered when only small amounts of intraoral autogenous bone graft are available. [source] Novel ceramic bone replacement material CeraBall® seeded with human mesenchymal stem cellsCLINICAL ORAL IMPLANTS RESEARCH, Issue 3 2010Timothy Douglas Abstract Objectives: Hydroxyapatite (HA) and tricalcium phosphate (TCP) are two very common ceramic materials for bone replacement. A recently developed material for bone replacement is CeraBall®, which is a mixed HA,TCP scaffold available as porous spherical scaffolds of diameter 4 and 6 mm. Before their use as bone replacement materials in vivo, in vitro testing of these scaffolds is necessary. The goal of this study was to characterise 4 and 6 mm CeraBall® scaffolds in vitro with a view to their future use as bone replacement materials. Materials and methods: The proliferation of human mesenchymal stromal cells (hMSCs) seeded on CeraBall® scaffolds was evaluated quantitatively using the WST [Water soluble tetrazolium ((4-[3-(4- Iodophenyl)-2-(4-nitrophenyl)-2H-5-tetrazolio]-1, 3-benzene disulfonate)] test and qualitatively by scanning electron microscopy (SEM). In addition, the standard MTT [(3-(4, 5-Dimenthylthiazol-2-Y1)-2, 5-Diphenyltetrazolium bromide)] biocompatibility test and cell vitality staining were performed using hMSCs. CeraBall® scaffolds were also tested for their mechanical properties. Results: SEM and WST test results showed that hMSCs proliferated on CeraBall® scaffolds over the course of 9 days. Proliferation was similar to that seen on tissue culture polystyrene (control). Cells showed a well-spread morphology and formed ,sheets' on the surface of scaffolds. Invasion of pores was observed. Good biocompatibility was demonstrated by MTT test results and cell vitality staining. Scaffolds of both 4 and 6 mm were able to withstand compressive loads of 5 N. Conclusions: CeraBall® scaffolds show good biocompatibility in vitro for hMSCs. This opens the way for in vivo applications. To cite this article: Douglas T, Liu Q, Humpe A, Wiltfang J, Sivananthan S, Warnke PH. Novel ceramic bone replacement material CeraBall® seeded with human mesenchymal stem cells. Clin. Oral Impl. Res. 21, 2010; 262,267. doi: 10.1111/j.1600-0501.2009.01818.x [source] Phase Relations Between ,-Tricalcium Phosphate and Hydroxyapatite with Manganese(II): Structural and Spectroscopic PropertiesEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 7 2006Isaac Mayer Abstract The preparation of Mn-containing ,-tricalcium phosphate (,-TCP) samples was achieved in two ways: a) transformation of precipitated Mn-containing calcium hydroxyapatite (HA) to ,-TCP by heating at 1100 °C, and b) preparation by solid-state reaction of a mixture of CaCO3, (NH4)2HPO4, and Mn(NO3)2 at 1100 °C. Powder X-ray diffraction (XRD) analyses of the samples, obtained by both methods, show well-defined patterns with structural data of the rhombohedral R3c, ,-TCP phase. The calculated lattice constants are smaller than those known for ,-Ca3(PO4)2 because of substitution of Ca2+ by Mn2+. EPR spectroscopy indeed reveals that manganese is divalent in the samples. Apparently, the Ca(5) site in the ,-TCP structure is occupied by Mn2+. The distribution of Mn2+ between the ,-TCP and the HA phase in the case of preparation (b) was studied by EPR spectroscopy, and a pronounced preference for the former lattice was found. Micron- and submicron-sized crystals with visible faces were observed by TEM in the case of ,-TCP prepared by solid-state reaction, and large micron-sized, droplike-shaped crystals, sensitive to beam radiation, were found in the case of samples prepared by heating HA at elevated temperatures. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006) [source] Fibronectin Functionalized Hydroxyapatite Coatings: Improving Dermal Fibroblast Adhesion In Vitro and In Vivo,ADVANCED ENGINEERING MATERIALS, Issue 8 2010Catherine J. Pendegrass Skin-penetrating devices including intraosseous transcutaneous amputation prostheses (ITAP) and external fixator pins rely on a skin-implant seal to prevent infection. In this study, we assess the effectiveness of fibronectin (Fn) functionalized hydroxyapatite (HA) coatings for promoting dermal fibroblast and dermal tissue attachment and ingrowth in vitro and in vivo. By measuring the number of focal adhesions per unit cell area we have demonstrated that HA significantly promotes dermal fibroblast attachment compared with titanium alloy. Dermal fibroblast attachment is promoted further using Fn functionalized HA coatings incorporated into an implant design with 700,µm pores, which significantly increased dermal tissue ingrowth and attachment compared with non-functionalized HA and titanium alloy controls incorporating 500 or 1000,µm pores. We postulate that Fn functionalized HA coatings applied to transdermal implants may promote and sustain the skin-implant interface and assist in preventing infection long term. [source] Biomimetic Carbonate,Hydroxyapatite Nanocrystals Prepared by Vapor Diffusion,ADVANCED ENGINEERING MATERIALS, Issue 7 2010Michele Iafisco Abstract Biomimetic carbonate,hydroxyapatite (HA) nanocrystals have been synthesized by using the sitting drop vapor diffusion technique, for the first time. The method consists of diffusing vapors of an aqueous solution of NH4HCO3 through drops containing an aqueous mixture of (CH3COO)2Ca and (NH4)2HPO4 in order to increase slowly their pH. This synthesis has been performed in a crystallization mushroom, a glass device developed for protein and small molecules crystallization. The concentrations of the reagents, the final pH and the crystallization time have been optimized to produce pure carbonate,HA as a single phase. X-Ray diffraction, Fourier transformed infrared spectroscopy, and transmission electron microscopy have been utilized to characterize the synthesized carbonated substituted HA crystals which display nanometric dimensions, plate-like morphology, and low crystallinity degree, closely resembling the inorganic phase of bones, teeth, and many pathological calcifications. This novel method may prove to be suitable for the study of the interactions and/or the co-crystallization of hydroxyapatite with minute amounts of biomolecules, polymers, or drugs. [source] Elaboration of Monophasic and Biphasic Calcium Phosphate Coatings on Ti6Al4V Substrate by Pulsed Electrodeposition CurrentADVANCED ENGINEERING MATERIALS, Issue 6 2010Hicham Benhayoune Calcium phosphate coatings on Ti6Al4V substrates are elaborated by pulsed electrodeposition. The surface morphology and chemical composition of the coatings are characterized by SEM,EDS. The obtained results are systematically confirmed at the nanometre scale using TEM. Moreover, XRD is performed in order to identify the coatings phases. The results show that pulsed electrodeposition allows uniform coatings to be obtained without the holes and craters usually observed with classical electrodeposition. After appropriate heat treatment, these coatings have a biphasic composition of stoichiometric hydroxyapatite and , -tricalcium phosphate. Moreover, the addition of 9% H2O2 to the electrolyte leads to monophasic coatings made of stoichiometric hydroxyapatite. As an indication of the passive nature of the electrodeposited coating, electrochemical potentiodynamic tests are performed in physiological solution in order to determine the corrosion behaviour of these coatings. [source] | ||||||||||||||||||||||||||||||||||